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nsv6462074

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:519

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 29 studies. See in: genome view    
    Submitted genomic60,329,949-60,330,467Question Mark
    Overlapping variant regions from other studies: 94 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):60,097,422-60,097,940Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6462074Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1160,329,94960,330,467
    nsv6462074RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1160,097,42260,097,940

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992502deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992502Submitted genomicNC_000011.10:g.603
    29949_60330467del
    GRCh38 (hg38)NC_000011.10Chr1160,329,94960,330,467
    nssv17992502RemappedPerfectNC_000011.9:g.6009
    7422_60097940del
    GRCh37.p13First PassNC_000011.9Chr1160,097,42260,097,940

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv179925020.033128138716
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